A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741764



Internal ID165430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102876000..102882542hg38UCSC Ensembl
chrX:102130928..102137470hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg386543
hg196543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138070
Supporting Variants
Samples
Known GenesLINC00630
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741764
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000844773


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